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Merck
CN

00930585

常春藤苷 C

primary reference standard

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关于此项目

经验公式（希尔记法）:
C59H96O26
化学文摘社编号:
14216-03-6
分子量:
1221.38
UNSPSC Code:
85151701
NACRES:
NA.24
PubChem Substance ID:
329747167
EC Number:
238-072-2
Beilstein/REAXYS Number:
4229541
MDL number:
MFCD00198062

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InChI key

RYHDIBJJJRNDSX-WBOYGZCJSA-N

InChI

1S/C59H96O26/c1-24-34(63)38(67)42(71)49(78-24)83-46-29(20-60)80-48(45(74)41(46)70)77-22-30-37(66)40(69)44(73)51(81-30)85-53(75)59-17-15-54(3,4)19-27(59)26-9-10-32-55(5)13-12-33(56(6,23-61)31(55)11-14-58(32,8)57(26,7)16-18-59)82-52-47(36(65)28(62)21-76-52)84-50-43(72)39(68)35(64)25(2)79-50/h9,24-25,27-52,60-74H,10-23H2,1-8H3/t24-,25-,27?,28-,29+,30+,31?,32+,33-,34-,35-,36-,37+,38+,39+,40-,41+,42+,43+,44+,45+,46+,47+,48+,49-,50-,51-,52-,55-,56-,57+,58+,59-/m0/s1

SMILES string

[H][C@]12CC=C3C4CC(C)(C)CC[C@@]4(CC[C@@]3(C)[C@]1(C)CCC5[C@](C)(CO)[C@H](CC[C@]25C)O[C@@H]6OC[C@H](O)[C@H](O)[C@H]6O[C@@H]7O[C@@H](C)[C@H](O)[C@@H](O)[C@H]7O)C(=O)O[C@@H]8O[C@H](CO[C@@H]9O[C@H](CO)[C@@H](O[C@@H]%10O[C@@H](C)[C@H](O)[C@@H](O)[C@H]%10O)[C@H](O)[C@H]9O)[C@@H](O)[C@H](O)[C@H]8O

grade

primary reference standard

shelf life

limited shelf life, expiry date on the label

manufacturer/tradename

HWI

mp

222 °C (dec.) (lit.)

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相关类别

General description

Produced and qualified by HWI pharma services GmbH.
Exact content by quantitative NMR can be found on the certificate.

Application

Reference Standard in the analysis of herbal medicinal products

Other Notes

This compound is commonly found in plants of the genus: hedera

pictograms

Exclamation mark
GHS07

signalword

Warning

hcodes

H302

Hazard Classifications

Acute Tox. 4 Oral

存储类别

11 - Combustible Solids

wgk

WGK 3

flash_point_f

No data available

flash_point_c

No data available

历史批次信息供参考:

分析证书(COA)

Lot/Batch Number
HWI02538
HWI02821
HWI02310-1
HWI02310
HWI02097

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Eun-Ha Joh et al.
Phytotherapy research : PTR, 26(4), 546-551 (2011-09-20)
The stem-bark of Kalopanax pictus (KP, family Araliaceae), which contains triterpenoid saponins, has been shown to exhibit anticarcinogenic, antiinflammatory, antirheumatoid and antidiabetic activities. In a preliminary study, a KP methanol extract demonstrated acetylcholinesterase activity in vitro and memory enhancement in
S H Cho et al.
Archives of pharmacal research, 14(1), 19-24 (1991-03-01)
One new triterpenoidal saponin, saponin F(2) has been isolated from the bark of Kalopanax pictum Nakai var. typicum (Araliaceae), together with one known saponin, kizuta saponin K12 (1). On the basis of chemico-spectral evidences, the structure of 2 has been
W J Sun et al.
Yao xue xue bao = Acta pharmaceutica Sinica, 25(1), 29-34 (1990-01-01)
Two crystalline components I and II were isolated from the total saponin of Kalopanax septemlobus (Thunb.) koidz. Crystalline II was identified as kalopanax saponin A and I was named as Kalopanax saponin C and eluciated as 3-O-[alpha-L-rhamnopyranosyl-(1----2)-alpha-L-arabinopyranosyl]- hedragenin-28-[alpha-L-rhamnopyranosyl-(1----2)- beta-D-glucopyranosyl (1----6)-beta-D-glucopyransyl]ester
Eun-Ha Joh et al.
Cellular immunology, 279(1), 103-108 (2012-11-03)
The stem bark of Kalopanax pictus Nakai (KP, family Araliaceae), of which main constituent is kalopanaxsaponin B, has been used for inflammation in Chinese traditional medicine. We isolated kalopanaxsaponin B from KP and investigated its anti-inflammatory effect in lipopolysaccharide (LPS)-stimulated
D H Kim et al.
Biological & pharmaceutical bulletin, 21(4), 360-365 (1998-05-20)
To investigate the relationship between the intestinal bacterial metabolism of kalopanaxsaponin B and H from Kalopanax pictus (Araliaceae), and their antidiabetic effect, kalopanaxsaponin B and H were metabolized by human intestinal microflora and the antidiabetic activity of their metabolites was
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Quantitative NMR for Content Assignment of Phytochemical Reference Standards

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